|Event Date/Time: Oct 17, 2011||End Date/Time: Oct 20, 2011|
Pharmacovigilance Asia 2011 is an unique learning platform that will bring together regulators as well as practitioners from the industry to discuss the ongoing pressing issues faced in drug safety, risk management, timeline constraints and varied regulatory standards. A featured panel of experts from the US and Europe will also be invited to provide you with key learning opportunities.
Key Benefits for Attending Pharmacovigilance Asia 2011
â€¢ Join the one and only conference platform for both pharmacovigliance regulators and industry practitioners
â€¢ Hear from an excellent panel of mixed speakers from both Asia and developed countries including the US and Europe
â€¢ Learn about pharmacovigilance and drug safety in Asia today, as well as the challenges and implications ahead to clinical trials and marketing
â€¢ Discuss best practices for both post-market and clinical stage pharmacovigilance
â€¢ Analyse different processes and methods for ADR case evaluation
â€¢ Exploring ways of developing and reinforcing a harmanised pharmacovigilance framework
What Delegates Say About our Past Events:
The very first event tailored on PV on a great Asian perspective!
â€“ PV Associate, Korea Otsuka
Simple enough to a beginner, complex enough for the experienced. Brilliant!
â€“ Senior Safety Officer, GSK
Very interesting with experienced key players
â€“ Head of Regional Center Pharmacovigilance, Boehringer Ingelheim
Very well organised conference. Attendees mix was nice â€“ including industry and regulators! Well done!
â€“ Head, Lifesciences EU & APAC, Cognizant
A great opportunity to network with peers in the region!
â€“ Associate Manager, Product Surveillance, Bausch & Lomb
This conference offers the opportunity for those working in pharmacovigilance to share expertise and learn about best practice and challenge the way they do things.
â€“ Pharmacovigliance Manager, MSD